Evidence map›Paper›PMID 21971153›Full record

ArticleEndocrinology2011

Cortistatin is not a somatostatin analogue but stimulates prolactin release and inhibits GH and ACTH in a gender-dependent fashion: potential role of ghrelin.

José Córdoba-Chacón, Manuel D Gahete, Ana I Pozo-Salas, Antonio J Martínez-Fuentes, Luis de Lecea, Francisco Gracia-Navarro, Rhonda D Kineman, Justo P Castaño, Raul M Luque

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 66 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

José Córdoba-ChacónDepartment of Cell Biology, University of Córdoba, Campus de Rabanales, Córdoba, Spain.
Manuel D Gahete
Ana I Pozo-Salas
Antonio J Martínez-Fuentes
Luis de Lecea
Francisco Gracia-Navarro
Rhonda D Kineman
Justo P Castaño
Raul M Luque
Centro de Investigación Biomédica en Red · ESUniversity of Córdoba · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESStanford University · USUniversity of Illinois Chicago · US

Funding

Interrelationship between the GH-axis and metabolismI01BX001114 · VA · JESSE BROWN VA MEDICAL CENTER · PI KINEMAN, RHONDA D · 2013 to 2016
–
BLRD VA I01 BX001114
6 · The paper itself

Abstract

Cortistatin (CST) and somatostatin (SST) evolve from a common ancestral gene and share remarkable structural, pharmacological, and functional homologies. Although CST has been considered as a natural SST-analogue acting through their shared receptors (SST receptors 1-5), emerging evidence indicates that these peptides might in fact exert unique roles via selective receptors [e.g. CST, not SST, binds ghrelin receptor growth hormone secretagogue receptor type 1a (GHS-R1a)]. To determine whether the role of endogenous CST is different from SST, we characterized the endocrine-metabolic phenotype of male/female CST null mice (cort-/-) at hypothalamic-pituitary-systemic (pancreas-stomach-adrenal-liver) levels. Also, CST effects on hormone expression/secretion were evaluated in primary pituitary cell cultures from male/female mice and female primates (baboons). Specifically, CST exerted an unexpected stimulatory role on prolactin (PRL) secretion, because both male/female cort-/- mice had reduced PRL levels, and CST treatment (in vivo and in vitro) increased PRL secretion, which could be blocked by a GHS-R1a antagonist in vitro and likely relates to the decreased success of female cort-/- in first-litter pup care at weaning. In contrast, CST inhibited GH and adrenocorticotropin-hormone axes in a gender-dependent fashion. In addition, a rise in acylated ghrelin levels was observed in female cort-/- mice, which were associated with an increase in stomach ghrelin/ghrelin O-acyl transferase expression. Finally, CST deficit uncovered a gender-dependent role of this peptide in the regulation of glucose-insulin homeostasis, because male, but not female, cort-/- mice developed insulin resistance. The fact that these actions are not mimicked by SST and are strongly gender dependent offers new grounds to investigate the hitherto underestimated physiological relevance of CST in the regulation of physiological/metabolic processes.

Indexed as

Adrenocorticotropic HormoneAnimalsFemaleGhrelinGrowth HormoneHypothalamic HormonesInsulinMaleMiceNeuropeptidesPapioProlactinSex FactorsSomatostatinAdrenocorticotropic HormonecortistatinGhrelinGrowth HormoneHypothalamic HormonesInsulinNeuropeptidesProlactinSomatostatin

Identifiers

PMID21971153
PMCPMC3230064
OpenAlexW2016391554

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.